SPAG9 (sperm associated antigen 9) - Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Gene: SPAG9 (sperm associated antigen 9) Homo sapiens
Analyze
Symbol: SPAG9
Name: sperm associated antigen 9
RGD ID: 1322667
HGNC Page HGNC:14524
Description: Predicted to enable kinesin binding activity; protein kinase binding activity; and signaling adaptor activity. Involved in lysosome localization and positive regulation of cell migration. Acts upstream of or within retrograde transport, endosome to Golgi. Located in centriolar satellite; cytosol; and lysosomal membrane. Implicated in hepatocellular carcinoma and liver cirrhosis. Biomarker of endometrial cancer.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: c-Jun NH2-terminal kinase-associated leucine zipper protein; C-Jun-amino-terminal kinase-interacting protein 4; cancer/testis antigen 89; CT89; FLJ13450; FLJ14006; FLJ26141; FLJ34602; HLC-6; HLC4; HLC6; human lung cancer oncogene 6 protein; JIP-4; JIP4; JLP; JNK interacting protein; JNK/SAPK-associated protein; KIAA0516; lung cancer oncogene 4; Max-binding protein; MGC117291; MGC14967; MGC74461; mitogen-activated protein kinase 8-interacting protein 4; PHET; PIG6; proliferation-inducing gene 6; protein highly expressed in testis; sperm associated antigen 9 variant 5; sperm surface protein; sperm-associated antigen 9; sunday driver 1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381750,962,174 - 51,120,868 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1750,962,174 - 51,120,868 (-)EnsemblGRCh38hg38GRCh38
GRCh371749,039,535 - 49,198,229 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361746,397,987 - 46,553,094 (-)NCBINCBI36Build 36hg18NCBI36
Build 341746,396,280 - 46,479,270NCBI
Celera1745,500,809 - 45,659,482 (-)NCBICelera
Cytogenetic Map17q21.33NCBI
HuRef1744,409,321 - 44,567,701 (-)NCBIHuRef
CHM1_11749,103,529 - 49,262,201 (-)NCBICHM1_1
T2T-CHM13v2.01751,829,515 - 51,988,191 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(1->4)-beta-D-glucan  (ISO)
(S)-nicotine  (EXP)
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
17beta-estradiol  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,6-dinitrotoluene  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-sulfonyldiphenol  (EXP)
acrolein  (EXP)
aflatoxin B1  (EXP,ISO)
all-trans-retinoic acid  (EXP,ISO)
alpha-pinene  (EXP)
arsenite(3-)  (EXP)
benzene  (EXP)
benzo[a]pyrene  (EXP,ISO)
bis(2-chloroethyl) sulfide  (EXP)
bisphenol A  (EXP,ISO)
Bisphenol B  (EXP)
bisphenol F  (EXP)
cadmium atom  (EXP)
caffeine  (EXP)
carbon nanotube  (ISO)
CGP 52608  (EXP)
chloroprene  (ISO)
choline  (ISO)
cisplatin  (EXP)
cobalt dichloride  (EXP)
copper atom  (ISO)
copper(0)  (ISO)
copper(II) sulfate  (EXP)
coumarin  (EXP)
crocidolite asbestos  (EXP)
crotonaldehyde  (EXP)
cyclosporin A  (EXP)
disodium selenite  (EXP)
diuron  (ISO)
dorsomorphin  (EXP)
entinostat  (EXP)
ethanol  (ISO)
folic acid  (ISO)
FR900359  (EXP)
fulvestrant  (EXP)
gentamycin  (ISO)
isoprenaline  (ISO)
ivermectin  (EXP)
L-methionine  (ISO)
lipopolysaccharide  (EXP)
methamphetamine  (ISO)
methyl methanesulfonate  (EXP)
methylmercury chloride  (EXP)
methylparaben  (EXP)
nicotine  (EXP)
oxaliplatin  (ISO)
ozone  (EXP,ISO)
panobinostat  (EXP)
paracetamol  (EXP,ISO)
perfluorooctane-1-sulfonic acid  (ISO)
pirinixic acid  (EXP)
resveratrol  (EXP)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
SB 431542  (EXP)
silicon dioxide  (EXP)
silver atom  (EXP)
silver(0)  (EXP)
sodium arsenate  (ISO)
streptozocin  (ISO)
succimer  (ISO)
sunitinib  (EXP)
testosterone enanthate  (EXP)
thimerosal  (EXP)
thioacetamide  (ISO)
topotecan  (EXP,ISO)
trichostatin A  (EXP)
tungsten  (ISO)
urethane  (EXP)
valproic acid  (EXP,ISO)
vorinostat  (EXP)
zinc atom  (EXP)
zinc(0)  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Sperm-associated antigen 9 is a promising marker for early diagnosis of endometrial cancer. Baser E, etal., Asian Pac J Cancer Prev. 2013;14(12):7635-8. doi: 10.7314/apjcp.2013.14.12.7635.
2. Mechanisms and functions of p38 MAPK signalling. Cuadrado A and Nebreda AR, Biochem J. 2010 Aug 1;429(3):403-17. doi: 10.1042/BJ20100323.
3. Serum levels of anti-sperm-associated antigen 9 antibody are elevated in patients with hepatocellular carcinoma. Ren B, etal., Oncol Lett. 2017 Dec;14(6):7608-7614. doi: 10.3892/ol.2017.7152. Epub 2017 Oct 9.
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9480848   PMID:9628581   PMID:10557099   PMID:12168954   PMID:12391307   PMID:12477932   PMID:14662895   PMID:14702039   PMID:14743216   PMID:15144186   PMID:15302935   PMID:15489334  
PMID:15693750   PMID:15923648   PMID:15987681   PMID:16077255   PMID:16112646   PMID:16344560   PMID:16356479   PMID:16959808   PMID:17081983   PMID:17353931   PMID:18029348   PMID:18826971  
PMID:18922895   PMID:19056739   PMID:19056867   PMID:19470755   PMID:19596235   PMID:19644450   PMID:19820019   PMID:19947555   PMID:20138665   PMID:20173330   PMID:20360068   PMID:21177868  
PMID:21282530   PMID:21356354   PMID:21873635   PMID:21900206   PMID:22146769   PMID:22522702   PMID:22586326   PMID:22863883   PMID:22939629   PMID:22990118   PMID:23376485   PMID:23696027  
PMID:23711689   PMID:24330581   PMID:24349057   PMID:24740566   PMID:24788963   PMID:24801907   PMID:24981860   PMID:25033008   PMID:25244576   PMID:25281560   PMID:25310386   PMID:25609649  
PMID:25659891   PMID:25921289   PMID:26186194   PMID:26291670   PMID:26293216   PMID:26468278   PMID:26631164   PMID:26790956   PMID:26797273   PMID:26831064   PMID:26934841   PMID:27173435  
PMID:27352556   PMID:27609421   PMID:27655714   PMID:27880917   PMID:28514442   PMID:28581483   PMID:28675297   PMID:28986522   PMID:29117863   PMID:29125462   PMID:29146937   PMID:29480665  
PMID:29507755   PMID:29540532   PMID:29676528   PMID:30110629   PMID:31091453   PMID:31300519   PMID:31485599   PMID:31586073   PMID:31690808   PMID:31815296   PMID:32017888   PMID:32235678  
PMID:32503577   PMID:32707033   PMID:32776977   PMID:32807901   PMID:32877691   PMID:33239621   PMID:33788575   PMID:33845483   PMID:33916271   PMID:33961781   PMID:34048709   PMID:34079125  
PMID:34319782   PMID:34380828   PMID:34597346   PMID:34709727   PMID:34795231   PMID:35013218   PMID:35140242   PMID:35256949   PMID:35271311   PMID:35439318   PMID:35446349   PMID:35831314  
PMID:35844135   PMID:35944360   PMID:36114006   PMID:36215168   PMID:36376293   PMID:36597993   PMID:36724073   PMID:36780531   PMID:37774976   PMID:38280479  


Genomics

Comparative Map Data
SPAG9
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381750,962,174 - 51,120,868 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1750,962,174 - 51,120,868 (-)EnsemblGRCh38hg38GRCh38
GRCh371749,039,535 - 49,198,229 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361746,397,987 - 46,553,094 (-)NCBINCBI36Build 36hg18NCBI36
Build 341746,396,280 - 46,479,270NCBI
Celera1745,500,809 - 45,659,482 (-)NCBICelera
Cytogenetic Map17q21.33NCBI
HuRef1744,409,321 - 44,567,701 (-)NCBIHuRef
CHM1_11749,103,529 - 49,262,201 (-)NCBICHM1_1
T2T-CHM13v2.01751,829,515 - 51,988,191 (-)NCBIT2T-CHM13v2.0
Spag9
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391193,886,794 - 94,016,919 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1193,886,917 - 94,016,911 (+)EnsemblGRCm39 Ensembl
GRCm381193,996,046 - 94,126,093 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1193,996,091 - 94,126,085 (+)EnsemblGRCm38mm10GRCm38
MGSCv371193,857,405 - 93,987,397 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361193,812,181 - 93,942,173 (+)NCBIMGSCv36mm8
Celera11103,596,032 - 103,742,397 (+)NCBICelera
Cytogenetic Map11DNCBI
cM Map1158.9NCBI
Spag9
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81079,440,311 - 79,574,709 (+)NCBIGRCr8
mRatBN7.21078,943,439 - 79,077,797 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1078,943,479 - 79,077,797 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1083,554,259 - 83,682,504 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01083,052,366 - 83,180,614 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01078,523,809 - 78,695,353 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01081,693,736 - 81,827,562 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1081,693,770 - 81,827,562 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01081,527,102 - 81,660,894 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41082,649,289 - 82,762,795 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11082,642,730 - 82,774,629 (+)NCBI
Celera1077,760,603 - 77,867,282 (+)NCBICelera
Cytogenetic Map10q26NCBI
Spag9
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495545110,800,128 - 10,895,400 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495545110,800,251 - 10,895,400 (+)NCBIChiLan1.0ChiLan1.0
SPAG9
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21967,150,865 - 67,309,121 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11771,957,919 - 72,116,131 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01745,053,292 - 45,211,488 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11749,924,650 - 50,081,918 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1749,924,650 - 50,081,918 (-)Ensemblpanpan1.1panPan2
SPAG9
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1926,820,381 - 26,966,315 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl926,820,002 - 26,966,300 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha926,148,726 - 26,294,511 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0927,613,837 - 27,760,017 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl927,613,700 - 27,760,276 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1926,380,745 - 26,526,372 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0926,639,936 - 26,785,790 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0926,769,987 - 26,915,874 (-)NCBIUU_Cfam_GSD_1.0
Spag9
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560226,278,463 - 26,425,767 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493649010,663,122 - 10,799,474 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493649010,663,155 - 10,796,658 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SPAG9
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1227,202,088 - 27,370,405 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11227,225,377 - 27,370,337 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21227,366,725 - 27,438,124 (-)NCBISscrofa10.2Sscrofa10.2susScr3
SPAG9
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11642,224,565 - 42,384,160 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1642,224,697 - 42,384,749 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607712,934,337 - 13,097,422 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Spag9
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247956,745,537 - 6,863,173 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247956,748,513 - 6,863,201 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SPAG9
58 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3		 pathogenic
GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3 copy number gain See cases [RCV000050957] Chr17:36449220..68170214 [GRCh38]
Chr17:48563237..65936105 [GRCh37]
Chr17:45918236..63677950 [NCBI36]
Chr17:17q21.33-24.2		 pathogenic
GRCh38/hg38 17q21.32-22(chr17:49137864-52147810)x1 copy number loss See cases [RCV000053432] Chr17:49137864..52147810 [GRCh38]
Chr17:47215226..50225170 [GRCh37]
Chr17:44570225..47580169 [NCBI36]
Chr17:17q21.32-22		 pathogenic
GRCh38/hg38 17q21.33-22(chr17:49974533-56807609)x1 copy number loss See cases [RCV000053433] Chr17:49974533..56807609 [GRCh38]
Chr17:48051897..54884970 [GRCh37]
Chr17:45406896..52239969 [NCBI36]
Chr17:17q21.33-22		 pathogenic
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3 copy number gain See cases [RCV000137437] Chr17:36449220..75053130 [GRCh38]
Chr17:57595736..73049225 [GRCh37]
Chr17:54950518..70560820 [NCBI36]
Chr17:17q23.1-25.1		 pathogenic
GRCh37/hg19 17q21.33-23.2(chr17:49076980-58740945)x3 copy number gain See cases [RCV000448805] Chr17:49076980..58740945 [GRCh37]
Chr17:17q21.33-23.2		 pathogenic
GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3 copy number gain See cases [RCV000447823] Chr17:42580684..81085615 [GRCh37]
Chr17:17q21.31-25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
NM_001130528.3(SPAG9):c.2756T>G (p.Phe919Cys) single nucleotide variant Inborn genetic diseases [RCV003290808] Chr17:50989734 [GRCh38]
Chr17:49067095 [GRCh37]
Chr17:17q21.33		 uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17q21.32-22(chr17:46481089-51396368)x1 copy number loss not provided [RCV000513510] Chr17:46481089..51396368 [GRCh37]
Chr17:17q21.32-22		 likely pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
NM_001130528.3(SPAG9):c.2813+6A>G single nucleotide variant not provided [RCV000924322] Chr17:50989671 [GRCh38]
Chr17:49067032 [GRCh37]
Chr17:17q21.33		 likely benign
NM_001130528.3(SPAG9):c.2058+9A>T single nucleotide variant not provided [RCV000924323] Chr17:50995435 [GRCh38]
Chr17:49072796 [GRCh37]
Chr17:17q21.33		 likely benign
NM_001130528.3(SPAG9):c.1476+10C>T single nucleotide variant not provided [RCV000974423] Chr17:51005202 [GRCh38]
Chr17:49082563 [GRCh37]
Chr17:17q21.33		 benign
NM_001130528.3(SPAG9):c.650C>T (p.Thr217Ile) single nucleotide variant Marfanoid habitus and intellectual disability [RCV000850425] Chr17:51041592 [GRCh38]
Chr17:49118953 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.3088+10G>A single nucleotide variant not provided [RCV000895835] Chr17:50984913 [GRCh38]
Chr17:49062274 [GRCh37]
Chr17:17q21.33		 benign
NM_001130528.3(SPAG9):c.2226+9G>A single nucleotide variant not provided [RCV000962597] Chr17:50995048 [GRCh38]
Chr17:49072409 [GRCh37]
Chr17:17q21.33		 benign
NM_001130528.3(SPAG9):c.1746G>A (p.Thr582=) single nucleotide variant not provided [RCV000979263] Chr17:50998536 [GRCh38]
Chr17:49075897 [GRCh37]
Chr17:17q21.33		 benign
NM_001130528.3(SPAG9):c.3114T>C (p.Tyr1038=) single nucleotide variant not provided [RCV000889794] Chr17:50982647 [GRCh38]
Chr17:49060008 [GRCh37]
Chr17:17q21.33		 benign
NM_001130528.3(SPAG9):c.2377C>T (p.Leu793=) single nucleotide variant not provided [RCV000889795] Chr17:50993785 [GRCh38]
Chr17:49071146 [GRCh37]
Chr17:17q21.33		 benign
NM_001130528.3(SPAG9):c.1745C>T (p.Thr582Met) single nucleotide variant Inborn genetic diseases [RCV003296135] Chr17:50998537 [GRCh38]
Chr17:49075898 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.1625C>T (p.Pro542Leu) single nucleotide variant Inborn genetic diseases [RCV003299696] Chr17:50999700 [GRCh38]
Chr17:49077061 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.1811C>A (p.Ser604Tyr) single nucleotide variant Inborn genetic diseases [RCV002990819] Chr17:50998471 [GRCh38]
Chr17:49075832 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.1446T>G (p.Asp482Glu) single nucleotide variant Inborn genetic diseases [RCV002901394] Chr17:51005242 [GRCh38]
Chr17:49082603 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.2882A>C (p.Glu961Ala) single nucleotide variant Inborn genetic diseases [RCV002773958] Chr17:50987169 [GRCh38]
Chr17:49064530 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.3805A>G (p.Met1269Val) single nucleotide variant Inborn genetic diseases [RCV002860397] Chr17:50970752 [GRCh38]
Chr17:49048113 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.904G>T (p.Val302Leu) single nucleotide variant Inborn genetic diseases [RCV002794214] Chr17:51021245 [GRCh38]
Chr17:49098606 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.1400G>A (p.Arg467Lys) single nucleotide variant Inborn genetic diseases [RCV002906986] Chr17:51006109 [GRCh38]
Chr17:49083470 [GRCh37]
Chr17:17q21.33		 likely benign
NM_001130528.3(SPAG9):c.67C>T (p.Arg23Trp) single nucleotide variant Inborn genetic diseases [RCV002732521] Chr17:51120590 [GRCh38]
Chr17:49197951 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.3775G>A (p.Glu1259Lys) single nucleotide variant Inborn genetic diseases [RCV002973243] Chr17:50970782 [GRCh38]
Chr17:49048143 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.722G>A (p.Arg241His) single nucleotide variant Inborn genetic diseases [RCV002945420] Chr17:51041520 [GRCh38]
Chr17:49118881 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.950T>C (p.Ile317Thr) single nucleotide variant Inborn genetic diseases [RCV002860363] Chr17:51021199 [GRCh38]
Chr17:49098560 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.2575C>A (p.Pro859Thr) single nucleotide variant Inborn genetic diseases [RCV002793392] Chr17:50990492 [GRCh38]
Chr17:49067853 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.2083T>G (p.Leu695Val) single nucleotide variant Inborn genetic diseases [RCV002869146] Chr17:50995200 [GRCh38]
Chr17:49072561 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.1853T>C (p.Leu618Ser) single nucleotide variant Inborn genetic diseases [RCV002849185] Chr17:50996680 [GRCh38]
Chr17:49074041 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.3133C>T (p.Arg1045Trp) single nucleotide variant Inborn genetic diseases [RCV002910939] Chr17:50982628 [GRCh38]
Chr17:49059989 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.859A>G (p.Thr287Ala) single nucleotide variant Inborn genetic diseases [RCV002951392] Chr17:51021290 [GRCh38]
Chr17:49098651 [GRCh37]
Chr17:17q21.33		 likely benign
NM_001130528.3(SPAG9):c.965C>A (p.Ala322Asp) single nucleotide variant Inborn genetic diseases [RCV002781772] Chr17:51021184 [GRCh38]
Chr17:49098545 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.336G>C (p.Gln112His) single nucleotide variant Inborn genetic diseases [RCV002869580] Chr17:51079672 [GRCh38]
Chr17:49157033 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.3671A>T (p.Asp1224Val) single nucleotide variant Inborn genetic diseases [RCV002912103] Chr17:50974800 [GRCh38]
Chr17:49052161 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.2790C>A (p.Asp930Glu) single nucleotide variant Inborn genetic diseases [RCV002874771] Chr17:50989700 [GRCh38]
Chr17:49067061 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.1846G>T (p.Ala616Ser) single nucleotide variant Inborn genetic diseases [RCV002713716] Chr17:50996687 [GRCh38]
Chr17:49074048 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.1466A>T (p.Asp489Val) single nucleotide variant Inborn genetic diseases [RCV002874639] Chr17:51005222 [GRCh38]
Chr17:49082583 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.1156C>G (p.Leu386Val) single nucleotide variant Inborn genetic diseases [RCV002827645] Chr17:51014289 [GRCh38]
Chr17:49091650 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.2081A>G (p.Asn694Ser) single nucleotide variant Inborn genetic diseases [RCV002666412] Chr17:50995202 [GRCh38]
Chr17:49072563 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.3539G>A (p.Gly1180Asp) single nucleotide variant Inborn genetic diseases [RCV002804770] Chr17:50974932 [GRCh38]
Chr17:49052293 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.316T>C (p.Phe106Leu) single nucleotide variant Inborn genetic diseases [RCV002930566] Chr17:51079692 [GRCh38]
Chr17:49157053 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.761C>T (p.Pro254Leu) single nucleotide variant Inborn genetic diseases [RCV002874746] Chr17:51031703 [GRCh38]
Chr17:49109064 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.505A>C (p.Asn169His) single nucleotide variant Inborn genetic diseases [RCV002718637] Chr17:51047460 [GRCh38]
Chr17:49124821 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.1921G>A (p.Gly641Ser) single nucleotide variant Inborn genetic diseases [RCV002831627] Chr17:50996612 [GRCh38]
Chr17:49073973 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.3571C>T (p.Arg1191Cys) single nucleotide variant Inborn genetic diseases [RCV002935697] Chr17:50974900 [GRCh38]
Chr17:49052261 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.2366A>G (p.Asn789Ser) single nucleotide variant Inborn genetic diseases [RCV002989217] Chr17:50993796 [GRCh38]
Chr17:49071157 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.2777A>G (p.Gln926Arg) single nucleotide variant Inborn genetic diseases [RCV002919905] Chr17:50989713 [GRCh38]
Chr17:49067074 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.3004T>G (p.Ser1002Ala) single nucleotide variant Inborn genetic diseases [RCV002854900] Chr17:50985714 [GRCh38]
Chr17:49063075 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.1948C>A (p.Leu650Met) single nucleotide variant Inborn genetic diseases [RCV002718141] Chr17:50996585 [GRCh38]
Chr17:49073946 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.1085G>A (p.Gly362Asp) single nucleotide variant Inborn genetic diseases [RCV002792296] Chr17:51020165 [GRCh38]
Chr17:49097526 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.857C>T (p.Ala286Val) single nucleotide variant Inborn genetic diseases [RCV002959475] Chr17:51021292 [GRCh38]
Chr17:49098653 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.3667C>T (p.Arg1223Trp) single nucleotide variant Inborn genetic diseases [RCV002747601] Chr17:50974804 [GRCh38]
Chr17:49052165 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.2161A>C (p.Thr721Pro) single nucleotide variant Inborn genetic diseases [RCV002897373] Chr17:50995122 [GRCh38]
Chr17:49072483 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.2690G>A (p.Gly897Glu) single nucleotide variant Inborn genetic diseases [RCV002722795] Chr17:50989800 [GRCh38]
Chr17:49067161 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.2599G>T (p.Val867Leu) single nucleotide variant Inborn genetic diseases [RCV003192002] Chr17:50990468 [GRCh38]
Chr17:49067829 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.1223G>A (p.Arg408Gln) single nucleotide variant Inborn genetic diseases [RCV003195005] Chr17:51007317 [GRCh38]
Chr17:49084678 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.3659A>G (p.His1220Arg) single nucleotide variant Inborn genetic diseases [RCV003181371] Chr17:50974812 [GRCh38]
Chr17:49052173 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.3085G>T (p.Val1029Leu) single nucleotide variant Inborn genetic diseases [RCV003183190] Chr17:50984926 [GRCh38]
Chr17:49062287 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.3070A>G (p.Ile1024Val) single nucleotide variant Inborn genetic diseases [RCV003200856] Chr17:50984941 [GRCh38]
Chr17:49062302 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.2191C>T (p.Gln731Ter) single nucleotide variant not provided [RCV003387649] Chr17:50995092 [GRCh38]
Chr17:49072453 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.721C>T (p.Arg241Cys) single nucleotide variant Inborn genetic diseases [RCV003368601] Chr17:51041521 [GRCh38]
Chr17:49118882 [GRCh37]
Chr17:17q21.33		 uncertain significance
NM_001130528.3(SPAG9):c.2780T>C (p.Ile927Thr) single nucleotide variant Inborn genetic diseases [RCV003383271] Chr17:50989710 [GRCh38]
Chr17:49067071 [GRCh37]
Chr17:17q21.33		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:5281
Count of miRNA genes:1375
Interacting mature miRNAs:1831
Transcripts:ENST00000262013, ENST00000357122, ENST00000502329, ENST00000505173, ENST00000505279, ENST00000506483, ENST00000506500, ENST00000509724, ENST00000510283, ENST00000510855, ENST00000511312, ENST00000511795, ENST00000511987, ENST00000513547, ENST00000513746, ENST00000513827, ENST00000513906, ENST00000514205, ENST00000514613, ENST00000515685, ENST00000576492
Prediction methods:Microtar, Miranda, Pita, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
WI-20746  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371749,039,577 - 49,039,782UniSTSGRCh37
Build 361746,394,576 - 46,394,781RGDNCBI36
Celera1745,500,851 - 45,501,056RGD
Cytogenetic Map17q21.33UniSTS
HuRef1744,409,363 - 44,409,568UniSTS
GeneMap99-GB4 RH Map17347.15UniSTS
Whitehead-RH Map17399.0UniSTS
NCBI RH Map17604.8UniSTS
RH44968  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371749,040,651 - 49,040,769UniSTSGRCh37
Build 361746,395,650 - 46,395,768RGDNCBI36
Celera1745,501,925 - 45,502,043RGD
Cytogenetic Map17q21.33UniSTS
HuRef1744,410,437 - 44,410,555UniSTS
GeneMap99-GB4 RH Map17347.15UniSTS
NCBI RH Map17604.8UniSTS
RH91778  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371749,043,046 - 49,043,231UniSTSGRCh37
Build 361746,398,045 - 46,398,230RGDNCBI36
Celera1745,504,320 - 45,504,505RGD
Cytogenetic Map17q21.33UniSTS
HuRef1744,412,832 - 44,413,017UniSTS
GeneMap99-GB4 RH Map17347.1UniSTS
RH76125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371749,039,578 - 49,039,783UniSTSGRCh37
Build 361746,394,577 - 46,394,782RGDNCBI36
Celera1745,500,852 - 45,501,057RGD
Cytogenetic Map17q21.33UniSTS
HuRef1744,409,364 - 44,409,569UniSTS
RH103888  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371749,102,857 - 49,102,939UniSTSGRCh37
Build 361746,457,856 - 46,457,938RGDNCBI36
Celera1745,564,105 - 45,564,187RGD
Cytogenetic Map17q21.33UniSTS
HuRef1744,472,591 - 44,472,673UniSTS
GeneMap99-GB4 RH Map17347.1UniSTS
SHGC-78834  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371749,045,519 - 49,045,789UniSTSGRCh37
Build 361746,400,518 - 46,400,788RGDNCBI36
Celera1745,506,793 - 45,507,063RGD
Cytogenetic Map17q21.33UniSTS
HuRef1744,415,305 - 44,415,575UniSTS
D17S819E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371749,109,238 - 49,109,342UniSTSGRCh37
GRCh371749,109,236 - 49,109,331UniSTSGRCh37
Build 361746,464,237 - 46,464,341RGDNCBI36
Celera1745,570,482 - 45,570,577UniSTS
Celera1745,570,484 - 45,570,588RGD
Cytogenetic Map17q21.33UniSTS
HuRef1744,478,970 - 44,479,074UniSTS
HuRef1744,478,968 - 44,479,063UniSTS
D17S1393E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371749,043,045 - 49,043,168UniSTSGRCh37
Build 361746,398,044 - 46,398,167RGDNCBI36
Celera1745,504,319 - 45,504,442RGD
Cytogenetic Map17q21.33UniSTS
HuRef1744,412,831 - 44,412,954UniSTS
D11S3862  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371163,620,395 - 63,620,674UniSTSGRCh37
GRCh371749,154,697 - 49,156,189UniSTSGRCh37
Build 361163,376,971 - 63,377,250RGDNCBI36
Celera1745,615,951 - 45,617,443UniSTS
Celera1160,946,273 - 60,946,552RGD
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map17q21.33UniSTS
HuRef1744,524,304 - 44,525,796UniSTS
HuRef1159,948,845 - 59,949,124UniSTS
D17S2022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371749,043,038 - 49,043,264UniSTSGRCh37
Build 361746,398,037 - 46,398,263RGDNCBI36
Celera1745,504,312 - 45,504,538RGD
Cytogenetic Map17q21.33UniSTS
HuRef1744,412,824 - 44,413,050UniSTS
Whitehead-YAC Contig Map17 UniSTS
RH12095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371749,040,130 - 49,040,305UniSTSGRCh37
Build 361746,395,129 - 46,395,304RGDNCBI36
Celera1745,501,404 - 45,501,579RGD
Cytogenetic Map17q21.33UniSTS
HuRef1744,409,916 - 44,410,091UniSTS
GeneMap99-GB4 RH Map17347.1UniSTS
NCBI RH Map17604.8UniSTS
RH78073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371749,042,536 - 49,042,690UniSTSGRCh37
Build 361746,397,535 - 46,397,689RGDNCBI36
Celera1745,503,810 - 45,503,964RGD
Cytogenetic Map17q21.33UniSTS
HuRef1744,412,322 - 44,412,476UniSTS
GeneMap99-GB4 RH Map17347.15UniSTS
NCBI RH Map17604.8UniSTS
STS-Z41139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371749,039,578 - 49,039,667UniSTSGRCh37
Build 361746,394,577 - 46,394,666RGDNCBI36
Celera1745,500,852 - 45,500,941RGD
Cytogenetic Map17q21.33UniSTS
HuRef1744,409,364 - 44,409,453UniSTS
GeneMap99-GB4 RH Map17347.1UniSTS
NCBI RH Map17604.8UniSTS
SHGC-30378  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371749,042,447 - 49,042,575UniSTSGRCh37
Build 361746,397,446 - 46,397,574RGDNCBI36
Celera1745,503,721 - 45,503,849RGD
Cytogenetic Map17q21.33UniSTS
HuRef1744,412,233 - 44,412,361UniSTS
Stanford-G3 RH Map172197.0UniSTS
GeneMap99-G3 RH Map172698.0UniSTS
D13S1553  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.2-q34.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map6p25.1UniSTS
D15S1390  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map7p13UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
D17S819E  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map17q21.33UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component
High
Medium 2334 2360 1515 416 1572 268 4348 1959 3679 370 1396 1598 162 1204 2785 4
Low 99 624 209 206 376 196 8 235 52 48 53 11 11 1 3
Below cutoff 2 2 2 1 1 3 1 7 2 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_029710 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001130527 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001130528 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001251971 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003971 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005257768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005257771 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005257774 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017025283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017025284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017025285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054317696 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054317697 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054317698 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054317699 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054317700 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054317701 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB011088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005839 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005920 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF327452 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF542172 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK023512 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK024068 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK129652 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295098 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299553 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302789 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307793 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY219897 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY219898 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY236487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY850123 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC007524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC059946 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC146755 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC153878 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA631864 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC332810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KJ624756 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC774920 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X91879 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000262013   ⟹   ENSP00000262013
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,962,174 - 51,120,868 (-)Ensembl
RefSeq Acc Id: ENST00000357122   ⟹   ENSP00000349636
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,965,644 - 51,120,865 (-)Ensembl
RefSeq Acc Id: ENST00000502329
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1751,031,443 - 51,047,471 (-)Ensembl
RefSeq Acc Id: ENST00000505173
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,989,639 - 51,056,424 (-)Ensembl
RefSeq Acc Id: ENST00000505279   ⟹   ENSP00000426900
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,965,627 - 51,120,734 (-)Ensembl
RefSeq Acc Id: ENST00000506483
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,993,773 - 50,995,960 (-)Ensembl
RefSeq Acc Id: ENST00000506500
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,966,300 - 50,975,360 (-)Ensembl
RefSeq Acc Id: ENST00000509724
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,964,149 - 50,965,494 (-)Ensembl
RefSeq Acc Id: ENST00000510283   ⟹   ENSP00000423165
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,965,075 - 51,046,878 (-)Ensembl
RefSeq Acc Id: ENST00000510855   ⟹   ENSP00000426061
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1751,021,252 - 51,046,878 (-)Ensembl
RefSeq Acc Id: ENST00000511312
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,976,600 - 50,982,672 (-)Ensembl
RefSeq Acc Id: ENST00000511795   ⟹   ENSP00000429343
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1751,001,837 - 51,020,259 (-)Ensembl
RefSeq Acc Id: ENST00000511987
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1751,030,914 - 51,046,837 (-)Ensembl
RefSeq Acc Id: ENST00000513547
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1751,001,835 - 51,016,256 (-)Ensembl
RefSeq Acc Id: ENST00000513746   ⟹   ENSP00000423346
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,974,870 - 50,990,585 (-)Ensembl
RefSeq Acc Id: ENST00000513827
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,996,229 - 51,001,745 (-)Ensembl
RefSeq Acc Id: ENST00000513906   ⟹   ENSP00000430205
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,985,699 - 50,993,937 (-)Ensembl
RefSeq Acc Id: ENST00000514205
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,990,023 - 50,990,742 (-)Ensembl
RefSeq Acc Id: ENST00000514613
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,989,540 - 51,079,622 (-)Ensembl
RefSeq Acc Id: ENST00000515685
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,998,413 - 51,001,744 (-)Ensembl
RefSeq Acc Id: ENST00000576492
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1751,007,269 - 51,040,451 (-)Ensembl
RefSeq Acc Id: ENST00000618113   ⟹   ENSP00000484908
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1750,962,174 - 51,120,865 (-)Ensembl
RefSeq Acc Id: NM_001130527   ⟹   NP_001123999
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381750,962,174 - 51,120,868 (-)NCBI
GRCh371749,039,535 - 49,198,226 (-)NCBI
HuRef1744,409,321 - 44,567,701 (-)NCBI
CHM1_11749,103,529 - 49,262,201 (-)NCBI
T2T-CHM13v2.01751,829,515 - 51,988,191 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001130528   ⟹   NP_001124000
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381750,962,174 - 51,120,868 (-)NCBI
GRCh371749,039,535 - 49,198,226 (-)ENTREZGENE
HuRef1744,409,321 - 44,567,701 (-)ENTREZGENE
CHM1_11749,103,529 - 49,262,201 (-)NCBI
T2T-CHM13v2.01751,829,515 - 51,988,191 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001251971   ⟹   NP_001238900
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381750,962,174 - 51,046,878 (-)NCBI
GRCh371749,039,535 - 49,198,226 (-)NCBI
HuRef1744,409,321 - 44,567,701 (-)NCBI
CHM1_11749,103,529 - 49,188,311 (-)NCBI
T2T-CHM13v2.01751,829,515 - 51,914,151 (-)NCBI
Sequence:
RefSeq Acc Id: NM_003971   ⟹   NP_003962
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381750,962,174 - 51,120,868 (-)NCBI
GRCh371749,039,535 - 49,198,226 (-)ENTREZGENE
Build 361746,397,987 - 46,553,094 (-)NCBI Archive
HuRef1744,409,321 - 44,567,701 (-)ENTREZGENE
CHM1_11749,103,529 - 49,262,201 (-)NCBI
T2T-CHM13v2.01751,829,515 - 51,988,191 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005257768   ⟹   XP_005257825
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381750,962,174 - 51,120,868 (-)NCBI
GRCh371749,039,535 - 49,198,226 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005257771   ⟹   XP_005257828
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381750,962,174 - 51,120,868 (-)NCBI
GRCh371749,039,535 - 49,198,226 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005257774   ⟹   XP_005257831
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381750,962,174 - 51,046,878 (-)NCBI
GRCh371749,039,535 - 49,198,226 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017025283   ⟹   XP_016880772
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381750,962,174 - 51,046,878 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017025284   ⟹   XP_016880773
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381750,962,174 - 51,046,878 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017025285   ⟹   XP_016880774
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381750,962,174 - 51,067,952 (-)NCBI
Sequence:
RefSeq Acc Id: XM_054317696   ⟹   XP_054173671
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01751,829,515 - 51,988,191 (-)NCBI
RefSeq Acc Id: XM_054317697   ⟹   XP_054173672
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01751,829,515 - 51,988,191 (-)NCBI
RefSeq Acc Id: XM_054317698   ⟹   XP_054173673
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01751,829,515 - 51,914,151 (-)NCBI
RefSeq Acc Id: XM_054317699   ⟹   XP_054173674
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01751,829,515 - 51,914,151 (-)NCBI
RefSeq Acc Id: XM_054317700   ⟹   XP_054173675
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01751,829,515 - 51,914,151 (-)NCBI
RefSeq Acc Id: XM_054317701   ⟹   XP_054173676
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01751,829,515 - 51,935,230 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001123999 (Get FASTA)   NCBI Sequence Viewer  
  NP_001124000 (Get FASTA)   NCBI Sequence Viewer  
  NP_001238900 (Get FASTA)   NCBI Sequence Viewer  
  NP_003962 (Get FASTA)   NCBI Sequence Viewer  
  XP_005257825 (Get FASTA)   NCBI Sequence Viewer  
  XP_005257828 (Get FASTA)   NCBI Sequence Viewer  
  XP_005257831 (Get FASTA)   NCBI Sequence Viewer  
  XP_016880772 (Get FASTA)   NCBI Sequence Viewer  
  XP_016880773 (Get FASTA)   NCBI Sequence Viewer  
  XP_016880774 (Get FASTA)   NCBI Sequence Viewer  
  XP_054173671 (Get FASTA)   NCBI Sequence Viewer  
  XP_054173672 (Get FASTA)   NCBI Sequence Viewer  
  XP_054173673 (Get FASTA)   NCBI Sequence Viewer  
  XP_054173674 (Get FASTA)   NCBI Sequence Viewer  
  XP_054173675 (Get FASTA)   NCBI Sequence Viewer  
  XP_054173676 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH07524 (Get FASTA)   NCBI Sequence Viewer  
  AAH59946 (Get FASTA)   NCBI Sequence Viewer  
  AAI46756 (Get FASTA)   NCBI Sequence Viewer  
  AAI53879 (Get FASTA)   NCBI Sequence Viewer  
  AAN61565 (Get FASTA)   NCBI Sequence Viewer  
  AAO66462 (Get FASTA)   NCBI Sequence Viewer  
  AAO66463 (Get FASTA)   NCBI Sequence Viewer  
  AAP74807 (Get FASTA)   NCBI Sequence Viewer  
  AAQ11383 (Get FASTA)   NCBI Sequence Viewer  
  AAX47276 (Get FASTA)   NCBI Sequence Viewer  
  AIC73822 (Get FASTA)   NCBI Sequence Viewer  
  BAA25442 (Get FASTA)   NCBI Sequence Viewer  
  BAB14812 (Get FASTA)   NCBI Sequence Viewer  
  BAG51202 (Get FASTA)   NCBI Sequence Viewer  
  BAG58134 (Get FASTA)   NCBI Sequence Viewer  
  BAG61498 (Get FASTA)   NCBI Sequence Viewer  
  BAG63993 (Get FASTA)   NCBI Sequence Viewer  
  BEO88559 (Get FASTA)   NCBI Sequence Viewer  
  CAA62987 (Get FASTA)   NCBI Sequence Viewer  
  EAW94569 (Get FASTA)   NCBI Sequence Viewer  
  EAW94570 (Get FASTA)   NCBI Sequence Viewer  
  EAW94571 (Get FASTA)   NCBI Sequence Viewer  
  EAW94572 (Get FASTA)   NCBI Sequence Viewer  
  EAW94573 (Get FASTA)   NCBI Sequence Viewer  
  EAW94574 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000262013
  ENSP00000262013.7
  ENSP00000349636
  ENSP00000349636.4
  ENSP00000423165
  ENSP00000423165.1
  ENSP00000423346.2
  ENSP00000426061.1
  ENSP00000426900
  ENSP00000426900.1
  ENSP00000429343.1
  ENSP00000430205.1
GenBank Protein O60271 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_003962   ⟸   NM_003971
- Peptide Label: isoform 3
- UniProtKB: O60271 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001124000   ⟸   NM_001130528
- Peptide Label: isoform 1
- UniProtKB: Q96II0 (UniProtKB/Swiss-Prot),   Q8IZX7 (UniProtKB/Swiss-Prot),   Q86WC8 (UniProtKB/Swiss-Prot),   Q86WC7 (UniProtKB/Swiss-Prot),   Q3MKM7 (UniProtKB/Swiss-Prot),   Q3KQU8 (UniProtKB/Swiss-Prot),   O60905 (UniProtKB/Swiss-Prot),   B4DHH2 (UniProtKB/Swiss-Prot),   A8MSX0 (UniProtKB/Swiss-Prot),   A6H8U5 (UniProtKB/Swiss-Prot),   Q9H811 (UniProtKB/Swiss-Prot),   O60271 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001123999   ⟸   NM_001130527
- Peptide Label: isoform 2
- UniProtKB: O60271 (UniProtKB/Swiss-Prot),   Q5JB53 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001238900   ⟸   NM_001251971
- Peptide Label: isoform 4
- UniProtKB: O60271 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005257828   ⟸   XM_005257771
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_005257825   ⟸   XM_005257768
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_005257831   ⟸   XM_005257774
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_016880773   ⟸   XM_017025284
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_016880774   ⟸   XM_017025285
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_016880772   ⟸   XM_017025283
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: ENSP00000426900   ⟸   ENST00000505279
RefSeq Acc Id: ENSP00000423165   ⟸   ENST00000510283
RefSeq Acc Id: ENSP00000426061   ⟸   ENST00000510855
RefSeq Acc Id: ENSP00000484908   ⟸   ENST00000618113
RefSeq Acc Id: ENSP00000429343   ⟸   ENST00000511795
RefSeq Acc Id: ENSP00000262013   ⟸   ENST00000262013
RefSeq Acc Id: ENSP00000430205   ⟸   ENST00000513906
RefSeq Acc Id: ENSP00000423346   ⟸   ENST00000513746
RefSeq Acc Id: ENSP00000349636   ⟸   ENST00000357122
RefSeq Acc Id: XP_054173672   ⟸   XM_054317697
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054173671   ⟸   XM_054317696
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054173676   ⟸   XM_054317701
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054173675   ⟸   XM_054317700
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054173674   ⟸   XM_054317699
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054173673   ⟸   XM_054317698
- Peptide Label: isoform X3
Protein Domains
JNK-interacting protein leucine zipper II   RH1   RH2

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O60271-F1-model_v2 AlphaFold O60271 1-1321 view protein structure

Promoters
RGD ID:6794003
Promoter ID:HG_KWN:26609
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000262013,   ENST00000357791,   ENST00000357804,   ENST00000376407,   NM_001130528,   NM_003971,   UC002ITD.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361746,552,976 - 46,553,552 (-)MPROMDB
RGD ID:7235683
Promoter ID:EPDNEW_H23588
Type:initiation region
Name:SPAG9_2
Description:sperm associated antigen 9
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23589  EPDNEW_H23590  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381751,046,878 - 51,046,938EPDNEW
RGD ID:7235687
Promoter ID:EPDNEW_H23589
Type:initiation region
Name:SPAG9_3
Description:sperm associated antigen 9
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23588  EPDNEW_H23590  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381751,120,753 - 51,120,813EPDNEW
RGD ID:7235689
Promoter ID:EPDNEW_H23590
Type:initiation region
Name:SPAG9_1
Description:sperm associated antigen 9
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23588  EPDNEW_H23589  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381751,120,865 - 51,120,925EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:14524 AgrOrtholog
COSMIC SPAG9 COSMIC
Ensembl Genes ENSG00000008294 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000262013 ENTREZGENE
  ENST00000262013.12 UniProtKB/Swiss-Prot
  ENST00000357122 ENTREZGENE
  ENST00000357122.8 UniProtKB/Swiss-Prot
  ENST00000505279 ENTREZGENE
  ENST00000505279.5 UniProtKB/Swiss-Prot
  ENST00000510283 ENTREZGENE
  ENST00000510283.5 UniProtKB/Swiss-Prot
  ENST00000510855.1 UniProtKB/TrEMBL
  ENST00000511795.1 UniProtKB/TrEMBL
  ENST00000513746.6 UniProtKB/TrEMBL
  ENST00000513906.1 UniProtKB/TrEMBL
Gene3D-CATH 1.20.58.1770 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.130.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  arf6 gtpase in complex with a specific effector, jip4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000008294 GTEx
HGNC ID HGNC:14524 ENTREZGENE
Human Proteome Map SPAG9 Human Proteome Map
InterPro JIP3/JIP4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  JIP_LZII UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  JNK/Rab-associated_protein-1_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RH1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RH2 UniProtKB/Swiss-Prot
  WD40/YVTN_repeat-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40_repeat_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:9043 UniProtKB/Swiss-Prot
NCBI Gene 9043 ENTREZGENE
OMIM 605430 OMIM
PANTHER C-JUN-AMINO-TERMINAL KINASE-INTERACTING PROTEIN 4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR13886 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam JIP_LZII UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Jnk-SapK_ap_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA37890 PharmGKB
PROSITE RH1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RH2 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF50978 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A060L980_HUMAN UniProtKB/TrEMBL
  A6H8U5 ENTREZGENE
  A8MSX0 ENTREZGENE
  B4DHH2 ENTREZGENE
  D6RHI8_HUMAN UniProtKB/TrEMBL
  H0Y981_HUMAN UniProtKB/TrEMBL
  H0YBE9_HUMAN UniProtKB/TrEMBL
  H0YBS5_HUMAN UniProtKB/TrEMBL
  JIP4_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  O60905 ENTREZGENE
  Q3KQU8 ENTREZGENE
  Q3MKM7 ENTREZGENE
  Q5JB53 ENTREZGENE, UniProtKB/TrEMBL
  Q86WC7 ENTREZGENE
  Q86WC8 ENTREZGENE
  Q8IZX7 ENTREZGENE
  Q96II0 ENTREZGENE
  Q9H811 ENTREZGENE
UniProt Secondary A6H8U5 UniProtKB/Swiss-Prot
  A8MSX0 UniProtKB/Swiss-Prot
  B4DHH2 UniProtKB/Swiss-Prot
  O60905 UniProtKB/Swiss-Prot
  Q3KQU8 UniProtKB/Swiss-Prot
  Q3MKM7 UniProtKB/Swiss-Prot
  Q86WC7 UniProtKB/Swiss-Prot
  Q86WC8 UniProtKB/Swiss-Prot
  Q8IZX7 UniProtKB/Swiss-Prot
  Q96II0 UniProtKB/Swiss-Prot
  Q9H811 UniProtKB/Swiss-Prot